Product NDC: | 50730-8304 |
Proprietary Name: | Triadine Scrub |
Non Proprietary Name: | povidone-iodine |
Active Ingredient(s): | .075 mL/mL & nbsp; povidone-iodine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50730-8304 |
Labeler Name: | Triad Group |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19850621 |
Package NDC: | 50730-8304-2 |
Package Description: | 118 mL in 1 BOTTLE (50730-8304-2) |
NDC Code | 50730-8304-2 |
Proprietary Name | Triadine Scrub |
Package Description | 118 mL in 1 BOTTLE (50730-8304-2) |
Product NDC | 50730-8304 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | povidone-iodine |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19850621 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Triad Group |
Substance Name | POVIDONE-IODINE |
Strength Number | .075 |
Strength Unit | mL/mL |
Pharmaceutical Classes |